CASEYS- benzalkonium chloride solution

Caseys by

Drug Labeling and Warnings

Caseys by is a Otc medication manufactured, distributed, or labeled by Zhejiang Bright Care Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient

BENZALKONIUM CHLORIDE 0.13%

PURPOSE

Purpose

Antibacterial

INDICATIONS & USAGE

Uses

• To decrease bacteria on the skin
• Recommended for repeated use

WARNINGS

Warnings

For external use only.

WHEN USING

When using this product, keep away from eyes.  In case of eye contact, rinse eyes with water

ASK DOCTOR

Stop use and ask a doctor if irritation or redness develops or lasts for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions:

• rub wipe thoroughly over all surfaces of both hands
• allow to dry without wiping
• superwise children under 6 years old
• not recommended for infants
• dispose of wipe in trash, do not flush

INACTIVE INGREDIENT

Inactive ingredients

Water, Fragrance, C12-15 Alcohols, Chloroxylenol, Aloe Barbadensis Leaf Juice

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CASEYS 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85844-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CHLOROXYLENOL (UNII: 0F32U78V2Q)
C12-15 ALCOHOLS (UNII: 2C8M6XLB5C)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85844-001-01	15 in 1 POUCH	08/30/2025
1		3.6 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	08/30/2025

Labeler - Zhejiang Bright Care Co., Ltd. (699496801)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Bright Care Co., Ltd.		699496801	manufacture(85844-001)